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HRID 482716作成日:2026年10月27日

p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime → 4-Chloro-benzaldehyde oxime

https://huagongshe.com/reaction/482716

反応式

関与物質

役割名称HCID仕込み量
反応物p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oximeHCID 85531600—
反応物HCID 178479532HCID 178479532—
生成物4-Chloro-benzaldehyde oximeHCID 219158—

反応手順

Using a similar procedure, 1-amino-3-p{[p-(1,1,2,2-tetrafluoroethoxy)benzylidene]amino}guanidine hydrochloride (white solid, mp 205°-212° C.); 1-amino-3-{p-(trifluoroethoxy)benzylidene]amino}guanidine hydrochloride (white powder; mp 235°-238° C.); and 1-amino-3-(p-chlorobenzylideneamino)guanidine hydrochloride may be prepared. The second products of the reactions, p-(1,1,2,2-tetrafluoroethoxy)benzaldehyde oxime (pinkish white solid, mp 47°-53.5° C.); α,α,α-trifluoro-p-anilaldehyde oxime (off-white solid, mp 46°-49.5° C.) and p-chlorbenzaldehyde oxime may also be isolated from the reactions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04575560
出典データセットuspto-grants-1986_03
ORD IDord-9fcc3b324f6b400e95029f008b8b7e70
出典メモuspto-grants-1986_03